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| Catalog: | GBAFP-CYP7B1-01859 |
| Classification: | Gene-specific Break Apart Probes |
| Description: | Our Gene-specific Break Apart Probes usually target the flanks of the target gene (CYP7B1). Due to this design method, our probe products can detect chromosomal rearrangements, such as translocations, by FISH.The product usually consists of a reagent combination composed of a probe with a selected dye color and a hybridization reagent. |
| Application: | CYP7B1 Gene-specific Break Apart Probe is designed to detect potential CYP7B1 rearrangements. This probe has been confirmed on the metaphase and interphase chromosomes by FISH. We provide a variety of dye color combinations for Break Apart Probes for customers to choose from. Probe products not only provide some classic color combinations, but also provide customized probe services. |
| Quantity: | 20 Tests |
| Probe Kits Volume (µL): | 40 μL |
| Hybridization Solution (µL): | 200 μL |
| Turnaround Time: | Within 10 Business Days |
| Shipping Time: | 1-2 Day Expedited Shipping |
| Shipping Conditions: | -20℃ |
| Storage Conditions: | Store at -20℃ and avoid light; |
| Gene Name | Cytochrome P450 Family 7 Subfamily B Member 1 |
| Gene Summary [Provided by RefSeq] | This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This endoplasmic reticulum membrane protein catalyzes the first reaction in the cholesterol catabolic pathway of extrahepatic tissues, which converts cholesterol to bile acids. This enzyme likely plays a minor role in total bile acid synthesis, but may also be involved in the development of atherosclerosis, neurosteroid metabolism and sex hormone synthesis. Mutations in this gene have been associated with hereditary spastic paraplegia (SPG5 or HSP), an autosomal recessive disorder. [provided by RefSeq, Apr 2016] |
| Gene Symbol | CYP7B1 |
| Location | 8q12.3 |
| Chromosome | Chromosome8 |
| Coordinates | This gene maps to 65508528-65711348 in GRCh37 coordinates. |
| Species | Human |
| Number | Dye Color | Order Name | Absorbance Maximum | Emission Maximum | Add to Cart |
| 1 | GR; OR | GBAFP-CYP7B1-01859-GROR | 515nm;573nm | 491nm;548nm | |
| 2 | AQ; OR | GBAFP-CYP7B1-01859-AQOR | 467nm;573nm | 418nm;548nm | |
| 3 | GO; GR | GBAFP-CYP7B1-01859-GOGR | 551nm;515nm | 525nm;491nm | |
| 4 | GO; RE | GBAFP-CYP7B1-01859-GORE | 551nm;599nm | 525nm;580nm | |
| 5 | GR; GO | GBAFP-CYP7B1-01859-GRGO | 515nm;551nm | 491nm;525nm | |
| 6 | GR; RE | GBAFP-CYP7B1-01859-GRRE | 515nm;599nm | 491nm;580nm | |
| 7 | OR; GR | GBAFP-CYP7B1-01859-ORGR | 573nm;515nm | 548nm;491nm | |
| 8 | RE; GO | GBAFP-CYP7B1-01859-REGO | 599nm;551nm | 580nm;525nm | |
| 9 | RE; GR | GBAFP-CYP7B1-01859-REGR | 599nm;515nm | 580nm;491nm |
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